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COAPROVEL TABS

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Coaprovel Tabs Adverse Events Reported to the FDA Over Time

How are Coaprovel Tabs adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Coaprovel Tabs, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Coaprovel Tabs is flagged as the suspect drug causing the adverse event.

Most Common Coaprovel Tabs Adverse Events Reported to the FDA

What are the most common Coaprovel Tabs adverse events reported to the FDA?

Renal Failure Acute
29 (4.14%)
Hyponatraemia
27 (3.86%)
Hyperkalaemia
16 (2.29%)
Fall
15 (2.14%)
Hypotension
14 (2%)
Malaise
14 (2%)
Vomiting
14 (2%)
Asthenia
13 (1.86%)
Confusional State
13 (1.86%)
Drug Interaction
12 (1.71%)
Hypokalaemia
11 (1.57%)
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Lactic Acidosis
11 (1.57%)
Dehydration
10 (1.43%)
Dizziness
10 (1.43%)
Bradycardia
9 (1.29%)
Renal Failure
9 (1.29%)
Diarrhoea
8 (1.14%)
Alanine Aminotransferase Increased
7 (1%)
Aspartate Aminotransferase Increase...
7 (1%)
Hepatitis
7 (1%)
Anaemia
6 (.86%)
Bone Marrow Failure
6 (.86%)
Circulatory Collapse
6 (.86%)
Hypertensive Crisis
6 (.86%)
Loss Of Consciousness
6 (.86%)
Pancreatitis Acute
6 (.86%)
Anorexia
5 (.71%)
Gamma-glutamyltransferase Increased
5 (.71%)
Nausea
5 (.71%)
Blood Creatinine Increased
4 (.57%)
Coma
4 (.57%)
Electrocardiogram Qrs Complex Prolo...
4 (.57%)
General Physical Health Deteriorati...
4 (.57%)
Inappropriate Antidiuretic Hormone ...
4 (.57%)
Orthostatic Hypotension
4 (.57%)
Pancytopenia
4 (.57%)
Pregnancy
4 (.57%)
Pyrexia
4 (.57%)
Vertigo
4 (.57%)
Weight Decreased
4 (.57%)
Weight Increased
4 (.57%)
Abdominal Pain Upper
3 (.43%)
Abortion Induced
3 (.43%)
Atrial Fibrillation
3 (.43%)
Atrioventricular Block Complete
3 (.43%)
Bone Sarcoma
3 (.43%)
Colitis
3 (.43%)
Cytolytic Hepatitis
3 (.43%)
Eczema
3 (.43%)
Epistaxis
3 (.43%)
Hypersensitivity
3 (.43%)
Infarction
3 (.43%)
Inflammation
3 (.43%)
Oedema Peripheral
3 (.43%)
Palpitations
3 (.43%)
Somnolence
3 (.43%)
Sudden Death
3 (.43%)
Temperature Intolerance
3 (.43%)
Therapeutic Agent Toxicity
3 (.43%)
Thrombocytopenia
3 (.43%)
Transaminases Increased
3 (.43%)
Urinary Tract Infection
3 (.43%)
Acidosis
2 (.29%)
Acute Generalised Exanthematous Pus...
2 (.29%)
Acute Respiratory Distress Syndrome
2 (.29%)
Agranulocytosis
2 (.29%)
Anxiety
2 (.29%)
Aphthous Stomatitis
2 (.29%)
Atrioventricular Block
2 (.29%)
Benign Prostatic Hyperplasia
2 (.29%)
Bicytopenia
2 (.29%)
Blood Alkaline Phosphatase Increase...
2 (.29%)
Blood Bilirubin Increased
2 (.29%)
Blood Glucose Fluctuation
2 (.29%)
Cholestasis
2 (.29%)
Condition Aggravated
2 (.29%)
Depressed Level Of Consciousness
2 (.29%)
Diabetes Mellitus Inadequate Contro...
2 (.29%)
Dialysis
2 (.29%)
Disorientation
2 (.29%)
Drug Exposure During Pregnancy
2 (.29%)
Dysphagia
2 (.29%)
Electrocardiogram Qt Prolonged
2 (.29%)
Eosinophilia
2 (.29%)
Extrapyramidal Disorder
2 (.29%)
Fatigue
2 (.29%)
Gastroenteritis
2 (.29%)
Hepatic Neoplasm Malignant
2 (.29%)
Hepatomegaly
2 (.29%)
Hyperammonaemia
2 (.29%)
Hypercalcaemia
2 (.29%)
Hyperparathyroidism
2 (.29%)
Hypertension
2 (.29%)
Hypoglycaemia
2 (.29%)
Hypoglycaemic Coma
2 (.29%)
Influenza
2 (.29%)
Interstitial Lung Disease
2 (.29%)
Ketoacidosis
2 (.29%)
Local Swelling
2 (.29%)
Medication Error
2 (.29%)
Metabolic Acidosis
2 (.29%)

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This graph shows the top adverse events submitted to the FDA for Coaprovel Tabs, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Coaprovel Tabs is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Coaprovel Tabs

What are the most common Coaprovel Tabs adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Coaprovel Tabs, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Coaprovel Tabs is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Coaprovel Tabs According to Those Reporting Adverse Events

Why are people taking Coaprovel Tabs, according to those reporting adverse events to the FDA?

Hypertension
121
Essential Hypertension
9
Cardiac Failure
2
Cardiac Failure Congestive
1
Aortic Valve Incompetence
1
Arrhythmia Supraventricular
1
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Suicide Attempt
1
Hypertensive Heart Disease
1

Coaprovel Tabs Case Reports

What Coaprovel Tabs safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

This report contains aggregated drug side effects and adverse events for Coaprovel Tabs. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

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